Variant report

Variant rs11905898
Chromosome Location chr20:14991701-14991702
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:14986600-14992600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr20:14986600-14993400 Weak transcription HepG2 liver
3 chr20:14986600-14996400 Weak transcription Ovary ovary
4 chr20:14988600-14992800 Weak transcription Cortex derived primary cultured neurospheres brain
5 chr20:14989200-14992000 Enhancers Fetal Intestine Small intestine
6 chr20:14991000-14993400 Enhancers Fetal Kidney kidney
7 chr20:14991600-14992000 Enhancers Gastric stomach
8 chr20:14991600-14993800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr20:14991600-14994200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
10 chr20:14991600-14994600 Enhancers Fetal Thymus thymus
11 chr20:14991600-14994800 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived

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